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“JSM” Peripheral Guide Wire - Taiwan Registration 0247f9fa278f1d21a59acf6d9559fdf6

Access comprehensive regulatory information for “JSM” Peripheral Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0247f9fa278f1d21a59acf6d9559fdf6 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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0247f9fa278f1d21a59acf6d9559fdf6
Registration Details
Taiwan FDA Registration: 0247f9fa278f1d21a59acf6d9559fdf6
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Device Details

“JSM” Peripheral Guide Wire
TW: “吉生”周邊血管導引線
Risk Class 2
MD

Registration Details

0247f9fa278f1d21a59acf6d9559fdf6

Ministry of Health Medical Device Manufacturing No. 004536

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E1330 Catheter Lead

Produced in Taiwan, China

Dates and Status

Feb 26, 2014

Feb 26, 2029